Defined metal atom aggregates precisely incorporated into metal–organic frameworks

金属有机骨架 纳米技术 纳米团簇 背景(考古学) 材料科学 计算机科学 化学 吸附 有机化学 生物 古生物学
作者
Kathrin L. Kollmannsberger,Laura Kronthaler,Joerg R. Jinschek,Roland A. Fischer
出处
期刊:Chemical Society Reviews [The Royal Society of Chemistry]
卷期号:51 (24): 9933-9959 被引量:41
标识
DOI:10.1039/d1cs00992c
摘要

Nanosized metal aggregates (MAs), including metal nanoparticles (NPs) and nanoclusters (NCs), are often the active species in numerous applications. In order to maintain the active form of MAs in "use", they need to be anchored and stabilised, preventing agglomeration. In this context, metal-organic frameworks (MOFs), which exhibit a unique combination of properties, are of particular interest as a tunable and porous matrix to host MAs. A high degree of control in the synthesis towards atom-efficient and application-oriented MA@MOF composites is required to derive specific structure-property relationships and in turn to enable design of functions on the molecular level. Due to the versatility of MA@MOF (derived) materials, their applications are not limited to the obvious field of catalysis, but increasingly include 'out of the box' applications, for example medical diagnostics and theranostics, as well as specialised (bio-)sensoring techniques. This review focuses on recent advances in the controlled synthesis of MA@MOF materials en route to atom-precise MAs. The main synthetic strategies, namely 'ship-in-bottle', 'bottle-around-ship', and approaches to achieve novel hierarchical MA@MOF structures are highlighted and discussed while identifying their potential as well as their limitations. Hereby, an overview of standard characterisation methods that enable a systematic analysis procedure and state-of-art techniques that localise MA within MOF cavities are provided. While the perspectives of MA@MOF materials in general have been reviewed various times in the recent past, few atom-precise MAs inside MOFs have been reported so far, opening opportunities for future investigation.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
田様应助眯眯眼的世界采纳,获得10
1秒前
筱筱发布了新的文献求助10
1秒前
1秒前
没有稗子完成签到 ,获得积分10
1秒前
2秒前
2秒前
JamesPei应助令狐剑通采纳,获得10
2秒前
zzd完成签到,获得积分10
2秒前
天天快乐应助圆圆采纳,获得10
2秒前
小秃子完成签到,获得积分10
3秒前
3秒前
浅尝离白应助yuan采纳,获得10
4秒前
xuhanghang完成签到,获得积分10
7秒前
直率向薇发布了新的文献求助50
7秒前
情怀应助中午采纳,获得10
7秒前
8秒前
9秒前
11秒前
Jasper应助罗汉果采纳,获得10
12秒前
大模型应助xiaolv采纳,获得10
12秒前
12秒前
13秒前
言不得语发布了新的文献求助10
13秒前
15秒前
桐桐应助Singularity采纳,获得10
16秒前
所所应助Ethan采纳,获得20
17秒前
整齐凌萱发布了新的文献求助10
18秒前
18秒前
筱筱发布了新的文献求助10
18秒前
il701发布了新的文献求助30
19秒前
骤雨时晴发布了新的文献求助10
20秒前
个性的雪旋完成签到 ,获得积分10
21秒前
令狐剑通发布了新的文献求助10
21秒前
中午发布了新的文献求助10
23秒前
aman007完成签到,获得积分10
23秒前
23秒前
FashionBoy应助乐乐乐乐乐乐采纳,获得10
24秒前
科研通AI2S应助11采纳,获得10
26秒前
顾子墨关注了科研通微信公众号
28秒前
高分求助中
Sustainability in Tides Chemistry 2800
Kinetics of the Esterification Between 2-[(4-hydroxybutoxy)carbonyl] Benzoic Acid with 1,4-Butanediol: Tetrabutyl Orthotitanate as Catalyst 1000
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
Rechtsphilosophie 1000
Handbook of Qualitative Cross-Cultural Research Methods 600
Very-high-order BVD Schemes Using β-variable THINC Method 568
Chen Hansheng: China’s Last Romantic Revolutionary 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3139127
求助须知:如何正确求助?哪些是违规求助? 2790013
关于积分的说明 7793363
捐赠科研通 2446416
什么是DOI,文献DOI怎么找? 1301093
科研通“疑难数据库(出版商)”最低求助积分说明 626106
版权声明 601102